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Treatment of myoclonic seizures in patients with juvenile myoclonic epilepsy

Authors Auvin S

Published 15 January 2008 Volume 2007:3(6) Pages 729—734

DOI https://doi.org/10.2147/NDT.S1107


Stéphane Auvin

Department of Pediatric Neurology, Lille University Hospital, Lille, France; Pharmacology Laboratory, Lille Medical School, Lille, France

Abstract: Drug treatment of Juvenile myoclonic epilepsy (JME) is mainly based on clinical experience and prospective and retrospective studies, with little evidence from randomized clinical trials. There are no head-to-head comparisons between old and new antiepileptic drugs (AEDs) and no drugs licensed specifically for JME. Valproate is unquestionably the drug of the first choice in men with JME. In women, lamotrigine should be preferred regarding teratogenicity and side effects of valproate. In addition, levetiracetam and topiramate are effective and can be use in combination or as second line treatment. Some AEDs can aggravate JME. In addition of AEDs, non-pharmacological treatments are important in JME. JME usually require lifelong treatment because seizures nearly always return after withdrawal of therapy.

Keywords: myoclonic seizure, myoclonic epilepsy, antiepileptic drugs

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